3,4-Dihydroxymandelic acid

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Names

[ CAS No. ]:
14883-87-5

[ Name ]:
3,4-Dihydroxymandelic acid

[Synonym ]:
MFCD00004231
3,4-Dihydroxy-DL-mandelic acid
rac-(R*)-Hydroxy(3,4-dihydroxyphenyl)acetic acid
DL-A,3,4-TRIHYDROXYPHENYLACETIC ACID
3,4-Dihydroxy-DL-ma
EINECS 238-956-8

Chemical & Physical Properties

[ Density]:
1.644g/cm3

[ Boiling Point ]:
487.5ºC at 760 mmHg

[ Melting Point ]:
136-137 °C (dec.)(lit.)

[ Molecular Formula ]:
C8H8O5

[ Molecular Weight ]:
184.14600

[ Flash Point ]:
262.7ºC

[ Exact Mass ]:
184.03700

[ PSA ]:
97.99000

[ LogP ]:
0.21580

[ Vapour Pressure ]:
2.57E-10mmHg at 25°C

[ Storage condition ]:
0-6°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Lipophilicity of amine neurotransmitter precursors, metabolites and related drugs estimated on various TLC plates.

J. Chromatogr. Sci. 52(9) , 1095-103, (2014)

The retention behavior for a series of amine neurotransmitters, their precursors, metabolites and structurally related drugs has been investigated in reversed-phase thin-layer chromatography using RP-...

Further study on the use of uncharged beta-cyclodextrin polymer in capillary electrophoresis: enantiomeric separation of some alpha-hydroxy acids.

Electrophoresis 16(8) , 1505-9, (1995)

Uncharged beta-cyclodextrin polymer was used as chiral selector for the enantiomeric separation of some alpha-hydroxy acids by capillary electrophoresis. Complexation and enantiomeric resolution of ma...

Mechanistic studies on tyrosinase-catalysed oxidative decarboxylation of 3,4-dihydroxymandelic acid.

Biochem. J. 281 ( Pt 2) , 353-7, (1992)

Mushroom tyrosinase, which is known to convert a variety of o-diphenols into o-benzoquinones, has been shown to catalyse an unusual oxidative decarboxylation of 3,4-dihydroxymandelic acid to 3,4-dihyd...


More Articles

Related Compounds

  • 3,4-Dihydroxymandelic acid
  • 3,4-dihydroxymandelic acid methyl ester
  • 3,4-Dichlorophenylboronic acid
  • 3,4-Dichlorobenzoic acid (1-(4-((3-amino-2,3,6-trideoxy-alpha-L-lyxo-hexopyranosyl)oxy)-1,2,3,4,6,11-hexahydro-2,5,12-trihydroxy-7-methoxy-6,11-dioxo-2-naphthacenyl)-2-hydroxyethylidene)hydrazide, mon
  • 3, 4-Dimethylbenzenesulfonic acid
  • 3,4 epoxybutyric acid
  • 4-Methoxy-N-methyl-I+/--phenylbenzenemethanamine
  • 8-Fluoro-4-methyl-2-piperazin-1-ylquinoline
  • Methyl 2-methyl-3-(1H-1,2,4-triazol-1-yl)propanoate
  • 1-[2-[(4-Bromophenyl)thio]-6-fluorophenyl]ethanone
  • Benzoic acid, 2-[(2-bromophenyl)thio]-5-nitro-
  • 2-[[(2-Bromophenyl)thio]methyl]benzonitrile
  • 1,3-benzothiazol-6-yl(1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)methanone
  • N-cyclopropylthieno[3,2-d]pyrimidin-4-amine
  • N-(3-morpholinopropyl)-5-(trifluoromethyl)pyridin-2-amine
  • N-(2-nitrophenyl)cycloheptanamine
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